NDC 24208-670

Sulfacetamide Sodium 100 mg per 1 mL solution/ drops

On the label: Bausch & Lomb Incorporated.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bausch & Lomb IncorporatedTampa, FL, United StatesMakes it Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action

Product details

Generic drug
Sulfacetamide: every company that makes it
Form
solution/ drops, ophthalmic
Strength
100 mg per 1 mL
Approval
ANDA ANDA040066
On the market since
Dec 28, 1994
Package NDCs
24208-670-04
Official label
DailyMed (National Library of Medicine), updated Aug 31, 2023

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